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Ergotamine adverse events reported to FDA.

Have You Experienced unusual Ergotamine symptoms? PatientsVille.com collects and analyzes Ergotamine side effect and adverse reports submitted by Ergotamine users, such as .

Summary

FDA Adverse Reports: 4. View All

Ergotamine FDA safety alerts: 2002 2007

Reported deaths: 2

Reported hospitalizations: 4

Ergotamine Dosage, Warnings, Usage.

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Often additional risks of using a medication, such as Ergotamine, become known after product is used by a larger number of patients, for a longer period of time, and by patients with different health characteristics from those studied before drug approval. This page allows You to Find answers and discuss health symptoms with other Ergotamine users, Learn more about unwanted side effects & find ways to reduce them. Browse Ergotamine Adverse Reports reported to FDA and participate in Ergotamine discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Ergotamine. You can also Post a question to users community or Ask a Doctor. PatientsVille.com is Your Complete Guide to all common, undocumented and undisclosed side effects associated with drugs and vaccines. Browse More Drug Reports Here: A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

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Ergotamine Adverse Effect Reports (FDA)

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7016107-9 | Ergot Poisoning, Peripheral Ischaemia
on Sep 14, 2010 Female patient from TURKEY , 18 years of age, was diagnosed with migraine (What is migraine?), upper respiratory tract infection and was treated with Ergotamine (View Usage). Patient experienced the following unwanted or unexpected effects: ergot poisoning, peripheral ischaemia. Ergotamine dosage: Unk. During the same period patient was treated with CLARITHROMYCIN (Unk) (View Clarithromycin Review and Clarithromycin Label ). Patient was hospitalized.

6932855-0 | Ergot Poisoning
Patient was taking Ergotamine (View Usage). Patient had the following side effects: ergot poisoning on Aug 09, 2010 from SWITZERLAND Additional patient health information: Male patient , 29 years of age, was diagnosed with migraine (What is migraine?), hiv infection (What is hiv infection?) and. Ergotamine dosage: 1 Mg, Daily. During the same period patient was treated with EMTRICITABINE W/TENOFOVIR (Unk) (View Emtricitabine W/tenofovir Review and Emtricitabine W/tenofovir Label ), LOPINAVIR AND RITONAVIR (Unk) (View Lopinavir And Ritonavir Review and Lopinavir And Ritonavir Label ). Patient was hospitalized.

6188713-5 | Vasospasm
Adverse event was reported on May 04, 2009 by a Female patient taking Ergotamine (View Usage) (Dosage: Unk) was diagnosed with headache (What is headache?) and. Location: SPAIN , 43 years of age, After Ergotamine was administered, patient had the following side effects: vasospasm. During the same period patient was treated with RITONAVIR (Unk) (View Ritonavir Review and Ritonavir Label ), TENOFOVIR (Unk) (View Tenofovir Review and Tenofovir Label ), EMTRICITABINE (Unk) (View Emtricitabine Review and Emtricitabine Label ), LOPINAVIR (Unk) (View Lopinavir Review and Lopinavir Label ). Patient was hospitalized.

6019698-X | Grand Mal Convulsion
on Dec 16, 2008 Female patient from FRANCE , 37 years of age, was diagnosed with migraine (What is migraine?) and was treated with Ergotamine (View Usage). Patient experienced the following unwanted or unexpected effects: grand mal convulsion. Ergotamine dosage: 2 Mg, Single.


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To find out about documented side effects or safety concerns read either the drug label or the drug's package insert. You may also want to speak with your pharmacist or healthcare provider. All medicines have benefits and risks. The risks are the chances that something unwanted or unexpected could happen to you when you use them. You can protect yourself by searching summaries of recent safety alerts, adverse reports. Sometimes there are risks that only come to light after a medical product gets on the market and is used in a larger number of patients, for a longer period of time, and in patients whose health characteristics are different from those of the patients studied before approval.

Be aware of the following potential Ergotamine risks to be aware of: 1. Watch for any Serious adverse events, such as life-threatening situation, which can require an admission to hospital or longer-than-expected hospital stay, permanent disability, birth defect, miscarriage, stillbirth, or birth with serious disease requires medical care to prevent permanent damage
2. Any potential Ergotamine quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Ergotamine use error: mixing up products with similar drug names or packaging, taking wrong dose of a drug because of confusing dosing instructions on label
4. When applicable, Problems with different manufacturer of same medicine: not getting same results from a generic drug as a brand name drug, or from another generic

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Ergotamine Reactions
Ergot Poisoning
Grand Mal Convulsion
Peripheral Ischaemia
Vasospasm
Ergotamine Side Effects Notice - The material on this site is for informational purposes only, and is not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. PatientsVille.com does not provide medical advice, diagnosis or treatment. The information regarding Ergotamine adverse reports, reviews and polls contained on PatientsVille.com site has not been scientifically or otherwise verified as to a cause and effect relationship and cannot be used to estimate the incidence of adverse drug reactions or for establishing or changing of patient treatments. Thank you for visiting Patientsville.com!